[go: up one dir, main page]

ATE136899T1 - METHOD FOR PRODUCING AN N-PHENYLACETYL DERIVATIVE OF TETRAHYDROTHIENO(3,2- C>PYRIDINE AND SYNTHESIS INTERMEDIATE - Google Patents

METHOD FOR PRODUCING AN N-PHENYLACETYL DERIVATIVE OF TETRAHYDROTHIENO(3,2- C>PYRIDINE AND SYNTHESIS INTERMEDIATE

Info

Publication number
ATE136899T1
ATE136899T1 AT91401891T AT91401891T ATE136899T1 AT E136899 T1 ATE136899 T1 AT E136899T1 AT 91401891 T AT91401891 T AT 91401891T AT 91401891 T AT91401891 T AT 91401891T AT E136899 T1 ATE136899 T1 AT E136899T1
Authority
AT
Austria
Prior art keywords
tetrahydrothieno
pyridine
producing
synthesis intermediate
phenylacetyl derivative
Prior art date
Application number
AT91401891T
Other languages
German (de)
Inventor
Marcel Descamps
Joel Radisson
Original Assignee
Sanofi Sa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9398542&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ATE136899(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Sa filed Critical Sanofi Sa
Application granted granted Critical
Publication of ATE136899T1 publication Critical patent/ATE136899T1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Process for the preparation of the compound of formula <IMAGE> characterised in that a formylating agent is reacted with the compound of formula <IMAGE> and in that the compounds formed are cyclised in the presence of an acid.
AT91401891T 1990-07-10 1991-07-08 METHOD FOR PRODUCING AN N-PHENYLACETYL DERIVATIVE OF TETRAHYDROTHIENO(3,2- C>PYRIDINE AND SYNTHESIS INTERMEDIATE ATE136899T1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR909008749A FR2664596B1 (en) 1990-07-10 1990-07-10 PROCESS FOR THE PREPARATION OF AN N-PHENYLACETIC DERIVATIVE OF TETRAHYDROTHIENO [3,2-C] PYRIDINE AND ITS SYNTHESIS INTERMEDIATE.

Publications (1)

Publication Number Publication Date
ATE136899T1 true ATE136899T1 (en) 1996-05-15

Family

ID=9398542

Family Applications (1)

Application Number Title Priority Date Filing Date
AT91401891T ATE136899T1 (en) 1990-07-10 1991-07-08 METHOD FOR PRODUCING AN N-PHENYLACETYL DERIVATIVE OF TETRAHYDROTHIENO(3,2- C>PYRIDINE AND SYNTHESIS INTERMEDIATE

Country Status (16)

Country Link
US (1) US5204469A (en)
EP (1) EP0466569B1 (en)
JP (1) JP2945174B2 (en)
KR (1) KR100198503B1 (en)
AT (1) ATE136899T1 (en)
AU (1) AU645816B2 (en)
CA (1) CA2046482C (en)
DE (1) DE69118765T2 (en)
DK (1) DK0466569T3 (en)
ES (1) ES2086505T3 (en)
FR (1) FR2664596B1 (en)
GR (1) GR3020434T3 (en)
HU (1) HU215957B (en)
IE (1) IE73222B1 (en)
PL (1) PL172216B1 (en)
PT (1) PT98244B (en)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI101150B (en) * 1991-09-09 1998-04-30 Sankyo Co Process for the preparation of tetrahydrothione nopyridine derivatives useful as a drug
US5334596A (en) * 1993-05-11 1994-08-02 Merck & Co., Inc. Fibrinogen receptor antagonists
US5576328A (en) * 1994-01-31 1996-11-19 Elf Sanofi Method for the secondary prevention of ischemic events
FR2760456B1 (en) * 1997-03-05 2000-05-12 Sanofi Sa PROCESS FOR THE PREPARATION OF 2-THIENYL-ETHYLAMINE DERIVATIVES
HU225503B1 (en) * 1997-05-13 2007-01-29 Sanofi Aventis Novel 2-(2-halophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides and process for producing them
HU222283B1 (en) * 1997-05-13 2003-05-28 Sanofi-Synthelabo Novel process for producing thieno[3,2-c]pyridine derivatives
HU225504B1 (en) * 1997-05-13 2007-01-29 Sanofi Aventis Novel halophenyl-(2-(2-thienyl)-ethylamino)-acetonitriles and process for producing them
FR2769313B1 (en) * 1997-10-06 2000-04-21 Sanofi Sa DERIVATIVES OF HYDROXYACETIC ESTERS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS SYNTHESIS INTERMEDIATES
HU226421B1 (en) * 1998-11-09 2008-12-29 Sanofi Aventis Process for racemizing optically active 2-(2-chlorophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides
WO2002018357A1 (en) * 2000-08-29 2002-03-07 Rpg Life Sciences Limited A ONE-POT PROCESS FOR THE PREPARATION OF PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS OF 4, 5, 6, 7 - TETRAHYDROTHIENO (3,2-c) PYRIDINE DERIVATIVES HAVING ANTITHROMBOTIC ACTIVITY
US6495691B1 (en) 2001-07-06 2002-12-17 Brantford Chemicals Inc. Process for the preparation of tetrahydrothieno[3,2-c]pyridine derivatives
US6767913B2 (en) 2001-12-18 2004-07-27 Teva Pharmaceutical Industries Ltd. Crystal forms iii, iv, v, and novel amorphous form of clopidogrel hydrogensulfate, processes for their preparation, processes for the preparation of form i, compositions containing the new forms and methods of administering the new forms
US7074928B2 (en) 2002-01-11 2006-07-11 Teva Pharmaceutical Industries, Ltd. Polymorphs of clopidogrel hydrogensulfate
HUP0200438A3 (en) * 2002-02-06 2003-10-28 Egis Gyogyszergyar Nyilvanosan Novel clopidogrel hydrochloride polymorphs, process for the preparation thereof, their use and pharmaceutical compositions containing them
ITMI20020933A1 (en) * 2002-05-03 2003-11-03 Danimite Dipharma S P A CLOPIDOGREL SYNTHESIS PROCEDURE
IL166593A0 (en) 2002-08-02 2006-01-15 Racemization and enantiomer separation of clopidogrel
US6800759B2 (en) * 2002-08-02 2004-10-05 Teva Pharmaceutical Industries Ltd. Racemization and enantiomer separation of clopidogrel
US6812363B2 (en) * 2002-10-15 2004-11-02 Usv Limited Racemization of optically active 2-substituted phenyl glycine esters
EP1606231A1 (en) * 2003-02-03 2005-12-21 Nadkarni, Sunil Sadanand Process for preparation of clopidogrel, its salts and pharmaceutical compositions
AU2003238664A1 (en) 2003-03-12 2004-09-30 Cadila Healthcare Limited Polymorphs and amorphous form of (s) - (+) -clopidogrel bisulfate
WO2004108665A2 (en) * 2003-04-24 2004-12-16 Sun Pharmaceutical Industries Limited A process for preparation of clopidogrel
GB0321256D0 (en) 2003-09-11 2003-10-08 Generics Uk Ltd Novel crystalline compounds
EP2103617A1 (en) 2003-11-03 2009-09-23 Cadila Healthcare Limited Processes for preparing different forms of (S)-(+)-clopidogrel bisulfate
CA2457459A1 (en) * 2004-02-11 2005-08-11 Brantford Chemicals Inc. Resolution of racemates of methyl alpha-5-(4,5,6,7-tetrahydro(3,2-c)thienopyridyl)-(2-chlorophenyl) acetate
KR100553398B1 (en) * 2004-03-12 2006-02-16 한미약품 주식회사 Process for preparing thieno [3,2-c] pyridine derivatives and intermediates used therein
WO2006003671A1 (en) * 2004-07-02 2006-01-12 Srinivasa Reddy Battula A process for resolution of methylamino(2-chlorophenyl)acetate
WO2007032023A2 (en) 2005-07-12 2007-03-22 Rpg Life Sciences Limited A process for preparation of methyl-(+)-(s)-alpha-(2-chlorophenyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4h)-acetic acid methyl ester or salts thereof having higher chiral purity and products thereof
JPWO2007026860A1 (en) * 2005-09-02 2009-03-12 第一ファインケミカル株式会社 Process for producing optically active α-hydroxycarboxylic acid
EP1942110A4 (en) * 2005-09-08 2010-08-04 Zhejiang Huahai Pharm Co Ltd Preparation of clopidogrel and its analogues methyl tetrahydrothienopyridine acetate compounds
CN100390180C (en) * 2005-12-15 2008-05-28 上海应用技术学院 Preparation method of clopidogrel and salt thereof
KR101235117B1 (en) * 2005-12-26 2013-02-20 에스케이케미칼주식회사 Process for the preparation of S-(+)-clopidogrel by optical resolution
US20070191609A1 (en) * 2006-02-13 2007-08-16 Lee Pharma Limited Process for preparation of clopidogrel bisulphate form-1
US20070225320A1 (en) * 2006-03-27 2007-09-27 Eswaraiah Sajja Process for preparing clopidogrel
WO2007144729A1 (en) * 2006-06-13 2007-12-21 Orchid Chemicals & Pharmaceuticals Limited An improved process for the preparation of clopidogrel
WO2008019053A2 (en) * 2006-08-03 2008-02-14 Teva Pharmaceutical Industries Ltd. Process for preparing clopidogrel bisulphate
ES2359851T3 (en) 2006-09-04 2011-05-27 Ranbaxy Laboratories Limited IMPROVED PROCESS FOR THE PREPARATION OF CLOPIDOGREL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS.
EP1980563A1 (en) 2007-04-09 2008-10-15 BATTULA, Srinivasa Reddy Procedure for the preparation of methyl (+)-(S)-Alpha-(O-chlorophenyl)-6,7-dihydrothieno-[3,2-C]pyridine-5(4H) acetate
WO2008130642A2 (en) * 2007-04-18 2008-10-30 Teva Pharmaceutical Industries Ltd. Improved process for preparing clopidogrel
KR100990949B1 (en) * 2008-06-09 2010-10-29 엔자이텍 주식회사 Method for preparing clopidogrel and its derivatives
WO2010046476A1 (en) * 2008-10-24 2010-04-29 Sandoz Ag A process for the preparation of s-clopidogrel
CN101434540B (en) * 2008-12-23 2011-07-20 重庆莱美药业股份有限公司 Method for synthesizing alpha-chlorine (2-chlorine) methyl phenyl acetate
CN101775001B (en) * 2010-01-28 2012-07-04 天津市中央药业有限公司 Method for synthesizing clopidogrel hydrogen sulfate intermediate by adopting solid acid catalytic esterification
CN102558138A (en) * 2010-12-08 2012-07-11 湖北成田制药股份有限公司 Preparation method for 2-halogenated phenyl-2-(2-thiophene diethylamino) acetic ester and salt thereof
WO2012123958A1 (en) 2011-02-14 2012-09-20 Cadila Healthcare Limited Highly pure salts of clopidogrel free of genotoxic impurities
CN103172527A (en) * 2011-12-26 2013-06-26 湖北德洲科技发展有限公司 Method for preparing clopidogrel synthetic intermediate-L-2-chlorophenylglycine methyl ester
CN103435631B (en) * 2013-08-29 2015-08-26 四川峨嵋山药业股份有限公司 The preparation method of I-type clopidogrel hydrogen sulfate
CN103483356B (en) * 2013-09-30 2016-01-13 浙江美诺华药物化学有限公司 A kind of preparation method of sulfate or hydrochloride of (S)-clopidogrel
CN108707156A (en) * 2018-08-03 2018-10-26 安徽省金楠医疗科技有限公司 Bisulfate clopidogrel synthetic method

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4127580A (en) * 1975-02-07 1978-11-28 Parcor Process for the preparation of thieno-pyridine derivatives
FR2397417A1 (en) * 1977-07-12 1979-02-09 Parcor PROCESS FOR PREPARATION OF THIENOPYRIDINE DERIVATIVES
FR2530247B1 (en) * 1982-07-13 1986-05-16 Sanofi Sa NOVEL THIENO (3, 2-C) PYRIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THERAPEUTIC APPLICATION
FR2623810B2 (en) * 1987-02-17 1992-01-24 Sanofi Sa ALPHA SALTS- (TETRAHYDRO-4,5,6,7 THIENO (3,2-C) PYRIDYL-5) (2-CHLORO-PHENYL) -THETHYL ACETATE DEXTROGYRE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
FR2624860B1 (en) * 1987-12-18 1990-06-01 Sanofi Sa PROCESS FOR THE PREPARATION OF N- (2-CHLORO-BENZYL) (THIENYL-2) -2 ETHYLAMINE
US4906756A (en) * 1988-05-10 1990-03-06 Syntex (U.S.A.) Inc. 2-(2-nitrovinyl)thiophene reduction and synthesis of thieno[3,2-c]pyridine derivatives
FR2652575B1 (en) * 1989-09-29 1992-01-24 Sanofi Sa PROCESS FOR THE PREPARATION OF ALPHA-BROMO PHENYLACETIC ACIDS.

Also Published As

Publication number Publication date
FR2664596A1 (en) 1992-01-17
PT98244B (en) 1998-12-31
DE69118765D1 (en) 1996-05-23
DE69118765T2 (en) 1996-10-24
FR2664596B1 (en) 1994-06-10
EP0466569B1 (en) 1996-04-17
IE912250A1 (en) 1992-01-15
JP2945174B2 (en) 1999-09-06
CA2046482A1 (en) 1992-01-11
KR100198503B1 (en) 1999-06-15
AU7949291A (en) 1992-01-16
PL290980A1 (en) 1992-06-26
AU645816B2 (en) 1994-01-27
ES2086505T3 (en) 1996-07-01
PL172216B1 (en) 1997-08-29
PT98244A (en) 1992-05-29
GR3020434T3 (en) 1996-10-31
JPH04230387A (en) 1992-08-19
HU215957B (en) 1999-03-29
DK0466569T3 (en) 1996-08-12
HU912311D0 (en) 1991-12-30
KR920002607A (en) 1992-02-28
HUT61556A (en) 1993-01-28
US5204469A (en) 1993-04-20
IE73222B1 (en) 1997-05-07
CA2046482C (en) 2001-10-30
EP0466569A1 (en) 1992-01-15

Similar Documents

Publication Publication Date Title
ATE136899T1 (en) METHOD FOR PRODUCING AN N-PHENYLACETYL DERIVATIVE OF TETRAHYDROTHIENO(3,2- C&gt;PYRIDINE AND SYNTHESIS INTERMEDIATE
ATE133950T1 (en) 2-THIENYLGLYCIDIC ACID DERIVATIVE, METHOD FOR THE PRODUCTION THEREOF AND ITS USE AS A SYNTHESIS INTERMEDIATE PRODUCT
ATE128961T1 (en) METHOD FOR PRODUCING PHENYLACETIC ACID DERIVATIVES FROM THIENOPYRIDINE AND INTERMEDIATE PRODUCTS OF ALPHA-BROMPHENYLACETIC ACIDS.
DE3775882D1 (en) SUBSTITUTED 6-FLUOR-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBONIC ACIDS; THEIR DERIVATIVES; PHARMACEUTICAL PREPARATIONS CONTAINING THIS COMPOUND AND METHOD FOR PRODUCING THESE COMPOUNDS.
HU9203761D0 (en) Method for producing substituted pyridine derivatives
DE3883456D1 (en) Process for the preparation of substituted indolinone derivatives.
DE3576952D1 (en) METHOD FOR PRODUCING 4-PHENYL-PYRROL DERIVATIVES.
DE69106003D1 (en) METHOD AND INTERMEDIATE PRODUCTS FOR THE PRODUCTION OF AZABICYCLO [2.2.2] OCTAN-3-IMINES.
HUT65340A (en) Process for producing 1,5-benzotriazepine derivatives
ATE156134T1 (en) METHOD FOR PRODUCING ALKYL POLYGLUCOSIDES
ATE229006T1 (en) METHOD FOR PRODUCING SULFUR-CONTAINING IMIDAZOLE DERIVATIVES AND INTERMEDIATE PRODUCTS OBTAINED
ATE189220T1 (en) METHOD FOR PRODUCING 7-(3-AMINO- AND 3-AMINOMETHYL-1-PYRROLIDINYL)-3-QUINOLOONE CARBOXYLIC ACIDS AND NAPHTHYRIDONE CARBOXYLIC ACIDS
DE3751149D1 (en) In position 3 2,2-dimethylcyclopropanecarboxylic acid derivatives substituted by a halogenated saturated chain, process for their preparation and their use for the production of pesticidal products.
ATE226570T1 (en) METHOD FOR PRODUCING HALOACETAMIDE DERIVATIVES
ATE127449T1 (en) ANILINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF.
ATE132863T1 (en) METHOD FOR PREPARING 6-(SUBSTITUTED AMINOPROPIONYL) DERIVATIVES OF FORSKOLIN
JPS5643287A (en) Preparation of cephamycin derivative
ATE156824T1 (en) METHOD FOR PRODUCING PYRIDO(1,2- A&gt;PYRIMIDINE DERIVATIVES
DE3878700D1 (en) METHOD FOR PRODUCING THIAZOLOBENZIMIDAZOLES AND INTERMEDIATE PRODUCTS.
DE69615570D1 (en) METHOD FOR PRODUCING CARBAMOYL METHYL URINE DERIVATIVES
JPS5576884A (en) 2-alylthiomethylene-1-oxapenam derivative and its preparation

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification
EELA Cancelled due to lapse of time